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Pilot Study: Cut the Cut – Evaluation of a treatment program for adolescents with nonsuicidal self-injury

Pilot Study: Cut the Cut – Evaluation of a treatment program for adolescents with nonsuicidal self-injury - E-CTC-P

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00016762
Enrollment
24
Registered
2019-03-05
Start date
2016-07-01
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nonsuicidal selfinjury (NSSI)

Interventions

Group 1: Patients were asked to fill the questionnaires FASM (Functional Assessment of Self-Mutilation), HIDS (How I deal with stress) and CSQ8 (Client Satisfaction Questionnaire) as well as answer a

Sponsors

ZfP Südwürttemberg, KJPP
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 17 Years

Inclusion criteria

Inclusion criteria: IQ>69; sufficient knowledge of German, age 14,0-17,11 years, Nonsuicidal self-injury as one of the reasons or the reason for inpatient admission

Exclusion criteria

Exclusion criteria: IQ<70; insufficient ability to speak German

Design outcomes

Primary

MeasureTime frame
Reduction of nonsuicidal self-injury, measured on a) the FASM (Functional Assessment of self-mutilation) and b) HIDS (How I deal with stress) as well as c) a 10 item semistructured interview. In the intervention group the FASM and HIDS will be administered at admission (T1), after interval one (T2) as well as upon completion of the interval program at interval three (T3). The interview will be administed at T2 and T3. In the control group the FASM and HIDS will be administered upon admission (T1) and discharge after inpatient treatment (T2). The interview will take place at T2.

Secondary

MeasureTime frame
Patient satisfaction with the treatment received will be evaluated on the consumer satisfaction questionnaire, short version (CSQ-8). In addition items on the semistructured interview refer to satisfaction. Data will be collected in the intervention group at T2 and T3, in the control group at T2.

Countries

Germany

Contacts

Public ContactIsabel Boege

ZfP Südwürttemberg, KJPP

Isabel.Boege@zfp-zentrum.de075176012789

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 23, 2026